Matches in Nanopublications for { ?s ?p "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 10 of
10
with 100 items per page.
- NP205668.RASCs2IXuwpd8qJ1JEw9WYSTaK9rCCMl6yGM1s1qKW5C0130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205668.RASCs2IXuwpd8qJ1JEw9WYSTaK9rCCMl6yGM1s1qKW5C0130_provenance.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.
- NP589364.RAViarDUYzk5DMQnAcaz1OuzqtYhRLoaoMJBu0huvv5fk130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589364.RAViarDUYzk5DMQnAcaz1OuzqtYhRLoaoMJBu0huvv5fk130_provenance.
- assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP663514.RAKF_5fYG-nFPVEWjBzzkAqyG5XoLwUuis_txl4c0XeUA130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663514.RAKF_5fYG-nFPVEWjBzzkAqyG5XoLwUuis_txl4c0XeUA130_provenance.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.
- NP593266.RAKhOR3MljN8B6uDF-N7qBcgfiKLIZTog2l2ccjwK9ZBk130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593266.RAKhOR3MljN8B6uDF-N7qBcgfiKLIZTog2l2ccjwK9ZBk130_provenance.